192188-39-9

Upstream product

• 192188-37-7 Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-(4-nitro-benzyloxycarbonylamino)-6-((2R,3R,4S,5R,6R)-4,5,6-tris-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-4-yl ester 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 4457-32-3 4-nitrobenzyl chloroformate 
• 192188-33-3 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-(4-nitro-benzyloxycarbonylamino)-6-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-4-yl ester 
• 192188-32-2 2-N-p-nitrobenzyloxycarbonyl-1,3,4,6-tetra-O-acetyl-D-glucosamine 
• 67831-42-9 benzyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Downstream Products

• 192188-41-3 (2R,3S,4R,5R,6S)-5-Amino-2-hydroxymethyl-6-((2R,3R,4S,5R,6R)-4,5,6-tris-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3,4-diol 

Relevant academic research and scientific papers

Use of the p-nitrobenzyloxycarbonyl group as an orthogonal amine protecting group in the synthesis of β-GlcNAc terminating glycosides

The p-nitrobenzyloxycarbonyl group serves as a participating group in the stereoselective formation of 2-amino-β-glucosides and as an N-protecting group which can be readily removed either by hydrogenolysis or by reaction with sodium dithionite under neut